专利 已放弃

USE OF CARRIPIYCIN IN MYCOBACTERIUM TUBERCULOSIS INFECTI0N RESISTANCE

Overview

本页收录老挝专利「USE OF CARRIPIYCIN IN MYCOBACTERIUM TUBERCULOSIS INFECTI0N RESISTANCE」的公开登记要点,由 SHENYANG FUYANG PHARMACEUTICAL TECHNOLOGY CO.,LTD。 于 2016-05-12 提交申请,当前状态为已放弃。公开档案中可核验:申请号 P/599,DIP 编号 LAP599,主管局代码 LA,保护类型 Patent - PCT National Phase。时间线要点:公开/公告日 2026-01-16。国际分类 / IPC 标注为 A61K 31/7048、A61P 31/06。发明人 / 设计人包括 HE, Weiqing、JIANG, Yang、WANG, Yiguang、ZHAO, Xiaofeng。代理机构 / 代理人记载为 CONCETTI-LAO CO., LTD。公开摘要提示:Use of carrimycin in mycobacterium tuberculosis infection resistance comprises the main steps: measuring the activity of carrimycin in myco…。

专利 老挝 DIP

申请号 P/599
申请日期 2016-05-12
申请人 SHENYANG FUYANG PHARMACEUTICAL TECHNOLOGY CO.,LTD。
代理机构 CONCETTI-LAO CO., LTD
类别 A61K 31/7048 · A61P 31/06

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基础信息

类型
专利
申请号
P/599
状态
已放弃
申请人
SHENYANG FUYANG PHARMACEUTICAL TECHNOLOGY CO.,LTD。
代理机构
CONCETTI-LAO CO., LTD
申请日期
2016-05-12
公开/公告日
2026-01-16
国际分类
A61K 31/7048 · A61P 31/06
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摘要

Use of carrimycin in mycobacterium tuberculosis infection resistance comprises the main steps: measuring the activity of carrimycin in mycobacterium tuberculosis resistance by adopting an absolute concentration method through taking clinical first-line antituberculotics, i.e., isoniazid and rifampicin as controls. The result indicates that carrimycin has obvious superior activity to clinically-separated mycobacterium tuberculosis including drug-resistant bacteria compared with those of the clinical first-line control drugs, i.e., the isoniazid and the rifampicin, and use of carrimycin in manufacturing drugs for treating tubercle bacillus infected diseases are expected to be developed.

Use of carrimycin in mycobacterium tuberculosis infection resistance comprises the main steps: measuring the activity of carrimycin in mycobacterium tuberculosis resistance by adopting an absolute concentration method through taking clinical first-line antituberculotics, i.e., isoniazid and rifampicin as controls. The result indicates that carrimycin has obvious superior activity to clinically-separated mycobacterium tuberculosis including drug-resistant bacteria compared with those of the clinical first-line control drugs, i.e., the isoniazid and the rifampicin, and use of carrimycin in manufacturing drugs for treating tubercle bacillus infected diseases are expected to be developed.

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